Canonical Allele Identifier: CA913190948

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 634792
• ClinVar RCV Id: RCV000785560
• dbSNP Id: rs1566231316

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32339250_32339293del , CM000675.2:g.32339250_32339293del	GRCh38
NC_000013.10:g.32913387_32913430del , CM000675.1:g.32913387_32913430del	GRCh37
NC_000013.9:g.31811387_31811430del	NCBI36
NG_012772.3:g.28771_28814del , LRG_293:g.28771_28814del

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.4895_4938del	ENSP00000434898.2:p.Ser1632AsnfsTer19
ENST00000528762.2:c.4895_4938del	ENSP00000433168.2:p.Ser1632AsnfsTer19
ENST00000530893.7:c.4526_4569del	ENSP00000499438.2:p.Ser1509AsnfsTer19
ENST00000665585.2:c.4895_4938del	ENSP00000499570.2:p.Ser1632AsnfsTer19
ENST00000666593.2:c.4895_4938del	ENSP00000499256.2:p.Ser1632AsnfsTer19
ENST00000700202.2:c.4895_4938del	ENSP00000514856.2:p.Ser1632AsnfsTer19
ENST00000380152.8:c.4895_4938del MANE Select	ENSP00000369497.3:p.Ser1632AsnfsTer19
ENST00000544455.6:c.4895_4938del	ENSP00000439902.1:p.Ser1632AsnfsTer19
ENST00000614259.2:c.4895_4938del	ENSP00000506251.1:p.Ser1632AsnfsTer19
ENST00000680887.1:c.4895_4938del	ENSP00000505508.1:p.Ser1632AsnfsTer19
ENST00000380152.7:c.4895_4938del	ENSP00000369497.3:p.Ser1632AsnfsTer19
ENST00000544455.5:c.4895_4938del	ENSP00000439902.1:p.Ser1632AsnfsTer19
ENST00000614259.1:n.4895_4938del
NM_000059.3:c.4895_4938del , LRG_293t1:c.4895_4938del	NP_000050.2:p.Ser1632AsnfsTer19
XM_011535203.1:c.4895_4938del	XP_011533505.1:p.Ser1632AsnfsTer19
XM_011535204.1:c.4895_4938del	XP_011533506.1:p.Ser1632AsnfsTer19
XM_011535205.1:c.4895_4938del	XP_011533507.1:p.Ser1632AsnfsTer19
NM_000059.4:c.4895_4938del MANE Select	NP_000050.3:p.Ser1632AsnfsTer19